FDA 510(k)

Trilor Disks, Blocks and Arches

Número K: K173643 · 2018-02-24

Data da decisão2018-02-24

Código do produtoEBF

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Trilor Disks, Blocks and Arches is the device name listed in this FDA 510(k) record. The listed applicant is Bioloren S.R.L.. It received FDA 510(k) clearance on 2018-02-24 under 510(k) number K173643. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Trilor Disks, Blocks and Arches?

Trilor Disks, Blocks and Arches is a medical device that received FDA 510(k) clearance on 2018-02-24. The listed applicant is Bioloren S.R.L.. The 510(k) number is K173643.

When did Trilor Disks, Blocks and Arches receive FDA 510(k) clearance?

Trilor Disks, Blocks and Arches received FDA 510(k) clearance on 2018-02-24, under 510(k) number K173643.

Who is the listed applicant for Trilor Disks, Blocks and Arches?

The FDA 510(k) record lists Bioloren S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Trilor Disks, Blocks and Arches?

The FDA product code for Trilor Disks, Blocks and Arches is EBF.

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Fonte oficial

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